Canonical Allele Identifier: CA2003527448

Gene: KMT2A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503135T= , CM000673.2:g.118503135T=	GRCh38
NC_000011.9:g.118373850T= , CM000673.1:g.118373850T=	GRCh37
NC_000011.8:g.117879060T=	NCBI36
NG_027813.1:g.71646T= , LRG_613:g.71646T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7342T=	ENSP00000432391.3:p.Ser2448=
ENST00000710560.1:c.7333T=	ENSP00000518343.1:p.Ser2445=
ENST00000649878.2:c.1282T=	ENSP00000497891.2:p.Ser428=
ENST00000685397.1:c.1282T=	ENSP00000509586.1:p.Ser428=
ENST00000686370.1:c.1282T=	ENSP00000509179.1:p.Ser428=
ENST00000689424.1:c.1540T=	ENSP00000509852.1:p.Ser514=
ENST00000691053.1:c.7315T=	ENSP00000509168.1:p.Ser2439=
ENST00000389506.10:c.7234T=	ENSP00000374157.5:p.Ser2412=
ENST00000528278.2:n.6585T=
ENST00000534358.8:c.7243T= MANE Select	ENSP00000436786.2:p.Ser2415=
ENST00000649699.1:c.7120T=	ENSP00000496927.1:p.Ser2374=
ENST00000389506.9:c.7234T=	ENSP00000374157.5:p.Ser2412=
ENST00000528278.1:n.1370T=
ENST00000534358.5:c.7243T=	ENSP00000436786.1:p.Ser2415=
NM_001197104.1:c.7243T= , LRG_613t1:c.7243T=	NP_001184033.1:p.Ser2415=
NM_005933.3:c.7234T=	NP_005924.2:p.Ser2412=
XM_006718839.2:c.4726T=	XP_006718902.2:p.Ser1576=
XM_011542829.1:c.7342T=	XP_011541131.1:p.Ser2448=
XM_011542830.1:c.7339T=	XP_011541132.1:p.Ser2447=
XM_011542831.1:c.7333T=	XP_011541133.1:p.Ser2445=
XM_011542832.1:c.5149T=	XP_011541134.1:p.Ser1717=
XM_011542833.1:c.4825T=	XP_011541135.1:p.Ser1609=
XM_006718839.3:c.4726T=	XP_006718902.2:p.Ser1576=
XM_011542829.2:c.7342T=	XP_011541131.1:p.Ser2448=
XM_011542830.2:c.7339T=	XP_011541132.1:p.Ser2447=
XM_011542831.2:c.7333T=	XP_011541133.1:p.Ser2445=
XM_011542833.2:c.4825T=	XP_011541135.1:p.Ser1609=
NM_001197104.2:c.7243T= MANE Select	NP_001184033.1:p.Ser2415=
NM_005933.4:c.7234T=	NP_005924.2:p.Ser2412=